Organometal catalyst compositions

ABSTRACT

This invention provides compositions that are useful for polymerizing at least one monomer to produce a polymer. This invention also provides compositions that are useful for polymerizing at least one monomer to produce a polymer, wherein said composition comprises a post-contacted organometal compound, a post-contacted organoaluminum compound, and a post-contacted treated solid oxide compound. The post-contacted organometal compound includes metallocenes. The post-contacted treated solid oxide compound contains fluorine, boron, and a solid oxide compound.

This application is a divisional application of U.S. patent applicationSer. No. 09/448,631, now U.S. Pat. No. 6,613,712, filed Nov. 24, 1999,which is incorporated herein in its entirety by reference.

FIELD OF THE INVENTION

This invention is related to the field of organometal catalystcompositions.

BACKGROUND OF THE INVENTION

The production of polymers is a multi-billion dollar business. Thisbusiness produces billions of pounds of polymers each year. Millions ofdollars have been spent on developing technologies that can add value tothis business.

One of these technologies is called metallocene catalyst technology.Metallocene catalysts have been known since about 1958. However, theirlow productivity did not allow them to be commercialized. About 1975, itwas discovered that contacting one part water with one parttrimethylaluminum to form methyl aluminoxane, and then contacting suchmethyl aluminoxane with a metallocene compound, formed a metallocenecatalyst that had greater activity. However, it was soon realized thatlarge amounts of expensive methyl aluminoxane were needed to form anactive metallocene catalyst. This has been a significant impediment tothe commercialization of metallocene catalysts.

Fluoro-organo borate compounds have been used in place of large amountsof methyl aluminoxane. However, this is not satisfactory, since suchborate compounds are very sensitive to poisons and decomposition, andcan also be very expensive.

It should also be noted that having a heterogeneous catalyst isimportant. This is because heterogeneous catalysts are required for mostmodern commercial polymerization processes. Furthermore, heterogeneouscatalysts can lead to the formation of substantially uniform polymerparticles that have a high bulk density. These types of substantiallyuniformed particles are desirable because they improve the efficiency ofpolymer production and transportation. Efforts have been made to produceheterogeneous metallocene catalysts; however, these catalysts have notbeen entirely satisfactory.

Therefore, the inventors provide this invention to help solve theseproblems.

SUMMARY OF THE INVENTION

An object of this invention is to provide a process that produces acatalyst composition that can be used to polymerize at least one monomerto produce a polymer.

Another object of this invention is to provide the catalyst composition.

Another object of this invention is to provide a process comprisingcontacting at least one monomer and the composition under polymerizationconditions to produce the polymer.

Another object of this invention is to provide an article that comprisesthe polymer produced with the catalyst composition of this invention.

In accordance with one embodiment of this invention, a process toproduce a catalyst composition is provided. The process comprises (oroptionally, “consists essentially of”, or “consists of”) contacting anorganometal compound, an organoaluminum compound, and a treated solidoxide compound to produce the catalyst composition,

wherein the organometal compound has the following general formula:(X¹)(X²)(X³)(X⁴)M¹

wherein M¹ is selected from the group consisting of titanium, zirconium,and hafnium;

wherein (X¹) is independently selected from the group consisting ofcyclopentadienyls, indenyls, fluorenyls, substituted cyclopentadienyls,substituted indenyls, and substituted fluorenyls;

wherein substituents on the substituted cyclopentadienyls, substitutedindenyls, and substituted fluorenyls of (X¹) are selected from the groupconsisting of aliphatic groups, cyclic groups, combinations of aliphaticand cyclic groups, silyl groups, alkyl halide groups, halides,organometallic groups, phosphorus groups, nitrogen groups, silicon,phosphorus, boron, germanium, and hydrogen;

wherein at least one substituent on (X¹) can be a bridging group whichconnects (X¹) and (X²);

wherein (X³) and (X⁴) are independently selected from the groupconsisting of halides, aliphatic groups, substituted aliphatic groups,cyclic groups, substituted cyclic groups, combinations of aliphaticgroups and cyclic groups, combinations of substituted aliphatic groupsand cyclic groups, combinations of aliphatic groups and substitutedcyclic groups, combinations of substituted aliphatic groups andsubstituted cyclic groups, amido groups, substituted amido groups,phosphido groups, substituted phosphido groups, alkyloxide groups,substituted alkyloxide groups, aryloxide groups, substituted aryloxidegroups, organometallic groups, and substituted organometallic groups;

wherein (X²) is selected from the group consisting of cyclopentadienyls,indenyls, fluorenyls, substituted cyclopentadienyls, substitutedindenyls, substituted fluorenyls, halides, aliphatic groups, substitutedaliphatic groups, cyclic groups, substituted cyclic groups, combinationsof aliphatic groups and cyclic groups, combinations of substitutedaliphatic groups and cyclic groups, combinations of aliphatic groups andsubstituted cyclic groups, combinations of substituted aliphatic groupsand substituted cyclic groups, amido groups, substituted amido groups,phosphido groups, substituted phosphido groups, alkyloxide groups,substituted alkyloxide groups, aryloxide groups, substituted aryloxidegroups, organometallic groups, and substituted organometallic groups;

wherein substituents on (X²) are selected from the group consisting ofaliphatic groups, cyclic groups, combinations of aliphatic groups andcyclic groups, silyl groups, alkyl halide groups, halides,organometallic groups, phosphorus groups, nitrogen groups, silicon,phosphorus, boron, germanium, and hydrogen;

wherein at least one substituent on (X²) can be a bridging group whichconnects (X¹) and (X²);

wherein the organoaluminum compound has the following general formula:Al(X⁵)_(n)(X⁶)_(3−n)

wherein (X⁵) is a hydrocarbyl having from 1 to about 20 carbon atoms;

wherein (X⁶) is a halide, hydride, or alkoxide; and

wherein “n” is a number from 1 to 3 inclusive;

wherein the treated solid oxide compound comprises fluorine, boron, anda solid oxide compound;

-   -   wherein the solid oxide compound comprises silica, and there is        a substantial absence of aluminum, titanium, or zirconium.

In accordance with another embodiment of this invention, a process isprovided comprising contacting at least one monomer and the catalystcomposition under polymerization condition to produce a polymer.

In accordance with another embodiment of this invention, an article isprovided. The article comprises the polymer produced in accordance withthis invention.

These objects, and other objects, will become more apparent to thosewith ordinary skill in the art after reading this disclosure.

DETAILED DESCRIPTION OF THE INVENTION

Organometal compounds used in this invention have the following generalformula:(X¹)(X²)(X³)(X⁴)M¹In this formula, M¹ is selected from the group consisting of titanium,zirconium, and hafnium. Currently, it is most preferred when M¹ iszirconium.

In this formula, (X¹) is independently selected from the groupconsisting of (hereafter “Group OMC-I”) cyclopentadienyls, indenyls,fluorenyls, substituted cyclopentadienyls, substituted indenyls, suchas, for example, tetrahydroindenyls, and substituted fluorenyls, suchas, for example, octahydrofluorenyls.

Substituents on the substituted cyclopentadienyls, substituted indenyls,and substituted fluorenyls of (X¹) can be selected independently fromthe group consisting of aliphatic groups, cyclic groups, combinations ofaliphatic and cyclic groups, silyl groups, alkyl halide groups, halides,organometallic groups, phosphorus groups, nitrogen groups, silicon,phosphorus, boron, germanium, and hydrogen, as long as these groups donot substantially, and adversely, affect the polymerization activity ofthe composition.

Suitable examples of aliphatic groups are hydrocarbyls, such as, forexample, paraffins and olefins. Suitable examples of cyclic groups arecycloparaffins, cycloolefins, cycloacetylenes, and arenes. Substitutedsilyl groups include, but are not limited to, alkylsilyl groups whereeach alkyl group contains from 1 to about 12 carbon atoms, arylsilylgroups, and arylalkylsilyl groups. Suitable alkyl halide groups havealkyl groups with 1 to about 12 carbon atoms. Suitable organometallicgroups include, but are not limited to, substituted silyl derivatives,substituted tin groups, substituted germanium groups, and substitutedboron groups.

Suitable examples of such substituents are methyl, ethyl, propyl, butyl,tert-butyl, isobutyl, amyl, isoamyl, hexyl, cyclohexyl, heptyl, octyl,nonyl, decyl, dodecyl, 2-ethylhexyl, pentenyl, butenyl, phenyl, chloro,bromo, iodo, trimethylsilyl, and phenyloctylsilyl.

In this formula, (X³) and (X⁴) are independently selected from the groupconsisting of (hereafter “Group OMC-II”) halides, aliphatic groups,substituted aliphatic groups, cyclic groups, substituted cyclic groups,combinations of aliphatic groups and cyclic groups, combinations ofsubstituted aliphatic groups and cyclic groups, combinations ofaliphatic groups and substituted cyclic groups, combinations ofsubstituted aliphatic and substituted cyclic groups, amido groups,substituted amido groups, phosphido groups, substituted phosphidogroups, alkyloxide groups, substituted alkyloxide groups, aryloxidegroups, substituted aryloxide groups, organometallic groups, andsubstituted organometallic groups, as long as these groups do notsubstantially, and adversely, affect the polymerization activity of thecomposition.

Suitable examples of aliphatic groups are hydrocarbyls, such as, forexample, paraffins and olefins. Suitable examples of cyclic groups arecycloparaffins, cycloolefins, cycloacetylenes, and arenes. Currently, itis preferred when (X³) and (X⁴) are selected from the group consistingof halides and hydrocarbyls, where such hydrocarbyls have from 1 toabout 10 carbon atoms. However, it is most preferred when (X³) and (X⁴)are selected from the group consisting of fluoro, chloro, and methyl.

In this formula, (X²) can be selected from either Group OMC-I or GroupOMC-II.

At least one substituent on (X¹) or (X²) can be a bridging group thatconnects (X¹) and (X²), as long as the bridging group does notsubstantially, and adversely, affect the activity of the composition.Suitable bridging groups include, but are not limited to, aliphaticgroups, cyclic groups, combinations of aliphatic groups and cyclicgroups, phosphorous groups, nitrogen groups, organometallic groups,silicon, phosphorus, boron, and germanium.

Suitable examples of aliphatic groups are hydrocarbyls, such as, forexample, paraffins and olefins. Suitable examples of cyclic groups arecycloparaffins, cycloolefins, cycloacetylenes, and arenes. Suitableorganometallic groups include, but are not limited to, substituted silylderivatives, substituted tin groups, substituted germanium groups, andsubstituted boron groups.

Various processes are known to make these organometal compounds. See,for example, U.S. Pat. Nos. 4,939,217; 5,210,352; 5,436,305; 5,401,817;5,631,335, 5,571,880; 5,191,132; 5,480,848; 5,399,636; 5,565,592;5,347,026; 5,594,078; 5,498,581; 5,496,781; 5,563,284; 5,554,795;5,420,320; 5,451,649; 5,541,272; 5,705,478; 5,631,203; 5,654,454;5,705,579; and 5,668,230; the entire disclosures of which are herebyincorporated by reference.

Specific examples of such organometal compounds are as follows:

bis(cyclopentadienyl)hafnium dichloride;

bis(cyclopentadienyl)zirconium dichloride;

1,2-ethanediylbis(η⁵-1-indenyl)di-n-butoxyhafnium;

1,2-ethanediylbis(η⁵-1-indenyl)dimethylzirconium;

3,3-pentanediylbis(η⁵-4,5,6,7-tetrahydro-1-indenyl)hafnium dichloride;

methylphenylsilylbis(η⁵-4,5,6,7-tetrahydro-1-indenyl)zirconiumdichloride;

bis(n-butylcyclopentadienyl)bis(di-t-butylamido)hafnium;

bis(n-butylcyclopentadienyl)zirconium dichloride;

dimethylsilylbis(1-indenyl)zirconium dichloride;

octylphenylsilylbis(1-indenyl)hafnium dichloride;

dimethylsilylbis(η⁵-4,5,6,7-tetrahydro-1-indenyl)zirconium dichloride;

dimethylsilylbis(2-methyl-1-indenyl)zirconium dichloride;

1,2-ethanediylbis(9-fluorenyl)zirconium dichloride;

indenyl diethoxy titanium(IV) chloride;

(isopropylamidodimethylsilyl)cyclopentadienyltitanium dichloride;

bis(pentamethylcyclopentadienyl)zirconium dichloride;

bis(indenyl) zirconium dichloride;

methyloctylsilyl bis(9-fluorenyl)zirconium dichloride;

and

bis-[1-(N,N-diisopropylamino)boratabenzene]hydridozirconiumtrifluoromethylsulfonate

Preferably, the organometal compound is selected from the groupconsisting of

bis(n-butylcyclopentadienyl)zirconium dichloride;

bis(indenyl)zirconium dichloride;

dimethylsilylbis(1-indenyl)zirconium dichloride;

and

methyloctylsilylbis(9-fluorenyl)zirconium dichloride

Organoaluminum compounds have the following general formula:Al(X⁵)_(n)(X⁶)_(3−n)In this formula, (X⁵) is a hydrocarbyl having from 1 to about 20 carbonatoms. Currently, it is preferred when (X⁵) is an alkyl having from 1 toabout 10 carbon atoms. However, it is most preferred when (X⁵) isselected from the group consisting of methyl, ethyl, propyl, butyl, andisobutyl.

In this formula, (X⁶) is a halide, hydride, or alkoxide. Currently, itis preferred when (X⁶) is independently selected from the groupconsisting of fluoro and chloro. However, it is most preferred when (X⁶)is chloro.

In this formula, “n” is a number from 1 to 3 inclusive. However, it ispreferred when “n” is 3.

Examples of such compounds are as follows:

trimethylaluminum;

triethylaluminum (TEA);

tripropylaluminum;

diethylaluminum ethoxide;

tributylaluminum;

diisobutylaluminum hydride;

triisobutylaluminum hydride;

triisobutylaluminum; and

diethylaluminum chloride.

Currently, TEA is preferred.

The treated solid oxide compound comprises fluorine, boron, and a solidoxide compound. The solid oxide compound comprises silica, and there isa substantial absence of titanium and zirconium.

Suitable preformed silicas include those made by aqueous gellation andsold commercially by W.R. Grace Company, such as Davison grade 952, andgrade 951, or flame hydrolyzed silicas such as those sold under the nameof Cabosils. Suitable silicas also include those made by aqueousgellation and subsequent drying from organic solvents, such asexemplified by U.S. Pat. No. 3,900,457, herein incorporated byreference. Suitable silicas may also be made by hydrolysis of ethyltetraorthosilicate provided that a gel thus formed is comprised ofsubstantially silica or silica-boria, as exemplified in U.S. Pat. Nos.4,301,034, 4,547,557, and 4,339,559; the entire disclosures of which areherein incorporated by reference.

To prepare the treated solid oxide compound, fluorine and boron can beadded to the solid oxide compound by any method known in the art. Inaddition, the fluorine and boron can be added to the solid oxidecompound in any order of steps that can produce the treated solid oxidecompound.

A boron-containing solid oxide compound can be made by aqueous oranhydrous cogellation of a silicate compound and a boron-containingcompound, or a preformed silica can be impregnated or otherwise treatedwith a boron-containing compound, such as, for example, boric acid,organic borate esters, boranes, alkyl boranes, and mixtures thereof. Aparticularly useful variation is to impregnate a preformed silica withammonium tetrafluoroborate (NH₄BF₄) or fluoroboric acid (HBF₄).

In a first method, the boron-containing solid oxide compound can be madeby any suitable method of cogelling boron from a boron-containingcompound and a silicate compound. The boron can be added to the solidoxide compound by cogellation of aqueous materials, as disclosed in U.S.Pat. Nos. 3,887,494; 3,119,569; 4,405,501; 4,436,882; 4,436,883;4,392,990; 4,081,407; 4,981,831; and 4,152,503; the entire disclosuresof which are hereby incorporated by reference. For example, ethyltetraorthosilicate can be reacted and hydrolyzed in the presence ofboric acid, a borate compound, or an organoboron compound to produce theboron-containing solid oxide compound. Alternatively, boron-containingcompounds, such as boric acid or sodium borates, can be incorporatedinto silicate gels formed from an aqueous water glass solution toproduce the boron-containing solid oxide compound.

In a second method, boron can be added to the solid oxide compound bycogellation in an organic or anhydrous solution as disclosed in U.S.Pat. Nos. 4,301,034; 4,547,557; and 4,339,559; the entire disclosures ofwhich are hereby incorporated by reference.

In a third method, silicon and boron compounds can be combined by flamehydrolysis.

The preferred method is to impregnate a preformed solid oxide compoundbefore or after calcining with an aqueous or organic solution of aboron-containing compound to produce the boron-containing solid oxidecompound. A suitable amount of the solution is utilized to provide thedesired concentration of boron after drying. The boron-containing solidoxide compound is then dried by any suitable method known in the art.For example, the drying can be accomplished by vacuum drying, spraydrying, or flash drying.

These boron-containing solid oxide compounds produced by cogellationcontain from about 0.5 to about 50% by weight boron based on the weightof the boron-containing solid oxide compound before calcining,preferably from about 1 to about 20 weight percent boron, and mostpreferably from 2 to 10 weight percent boron. The boron-containing solidoxide compounds can also contain minor amounts of other components,provided that the do not interfere with their use as an activator forthe organometal compounds. Other minor components include, but are notlimited to, iron, calcium, chromium, vanadium, zinc, nickel, phosphate,magnesium, and the like.

The solid oxide compound should have a pore volume greater than about0.5 cc/g, preferably greater than about 0.8 cc/g, and most preferably,greater than 1.0 cc/g.

The solid oxide compound should have a surface area after calcining at500° C. in a range of about 100 to about 1000 m²/g, preferably fromabout 200 to about 800 m²/g, and most preferably, from 250 to 600 m²/g.

Any boron-containing compound known in the art that can impregnate thesolid oxide compound with boron can be used in this invention. Theboron-containing compound can include, but is not limited to, boric acid(H₃BO₃), sodium borate (Na₃BO₃), boron propoxide (B(OC₃H₇)₃),triethylborane (B(C₂H₅)₃), boroxines, boron hydrides, and mixturesthereof.

When impregnating a preformed silica with a boron-containing compound,generally, the amount of boron present is in a range of about 0.1 toabout 10 millimoles per gram of boron-containing solid oxide compoundbefore calcining or the amount added to a precalcined solid oxidecompound. Preferably, the amount of boron present in theboron-containing solid oxide compound is in a range of about 0.5 toabout 5 millimoles per gram of boron-containing solid oxide compoundbefore calcining or the amount added to a precalcined solid oxidecompound. Most preferably, the amount of boron present is in a range of1 to 3 millimoles per gram of boron-containing solid oxide compoundbefore calcining or the amount added to a precalcined solid oxidecompound.

In at least one step in the production of the treated solid oxidecompound, calcining occurs. Generally, calcining is conducted for about1 minute to about 100 hours, preferably for about 1 hour to about 50hours, and most preferably, from 3 hours to 20 hours. The calcining isconducted at a temperature in a range of about 150 to about 900° C.,preferably, in a range of about 200 to about 700° C., and mostpreferably, in a range of 250 to 500° C. Any type of suitable atmospherecan be used during calcining. Generally, calcining can be completed inan inert atmosphere. Alternatively, an oxiding atmosphere, such as, forexample, oxygen or air, or a reducing atmosphere, such as, for example,hydrogen or carbon monoxide, can be used.

To produce the treated solid oxide compound, before, during, or aftercalcining, the solid oxide compound is contacted with afluorine-containing compound. Any method known in the art for contactingthe solid oxide compound with the fluorine-containing compound can beused in this invention. One common method is to impregnate the solidoxide compound with an aqueous solution of a fluorine-containing salt,such as, for example, ammonium fluoride (NH₄F), ammonium bifluoride(NH₄HF₂), hydrofluoric acid (HF), ammonium silicofluoride ((NH₄)₂SiF₆),ammonium fluoroborate (NH₄BF₄), ammonium fluorophosphate (NH₄PF₆),fluoroboric acid (HBF₄), and mixtures thereof. Alternatively, thefluorine-containing compound can be dissolved into an organic solvent,such as an alcohol, and used to impregnate the solid oxide compound tominimize shrinkage of pores during drying. Drying can be accomplished byany method known in the art such as vacuum drying, spray drying, flashdrying, and the like.

The fluorine-containing compound can also be incorporated into a gel byadding it to one of the aqueous materials before gellation. Theseaqueous materials were disclosed in the first and second methods forpreparing boron-containing solid oxide compounds discussed previously inthis disclosure.

The fluorine-containing compound can also be added to a slurrycontaining a gel before drying. Formation of a gel was disclosed in thefirst and second methods for preparing boron-containing solid oxidecompounds discussed previously in this disclosure.

The fluorine-containing compound can also be added during calcining. Inthis technique, the fluoride-containing compound can be vaporized into agas stream used to fluidize the solid oxide compound or boron-containingsolid oxide compound so that it is fluorided from the gas stream. Inaddition to some of the fluorine-containing compounds described above,volatile organic fluorides may be used at temperatures above theirdecomposition points, or at temperatures high enough to cause reaction.For example, perfluorohexane, perfluorobenzene, trifluoroacetic acid,trifluoroacetic anhydride, hexafluoroacetylacetonate, and mixturesthereof can be vaporized and contacted with the solid oxide compound orboron-containing solid oxide compound at about 300 to about 600° C. inair or nitrogen. Inorganic fluoride containing vapors may also be used,such as, for example, hydrogen fluoride or even elemental fluorine gas.

The solid oxide compound or boron-containing solid oxide compound canalso be calcined at a temperature in a range of about 100 to 900° C.before being fluorided.

Another method of producing the treated solid oxide compound is tosimultaneously contact a preformed solid oxide compound prior tocalcining with a boron-containing compound, such as boric acid, and afluorine-containing compound, such as hydrofluoric acid.

A preferred method of producing the treated solid oxide compound is tocontact a preformed solid oxide compound before calcining and ammoniumfluoroborate (NH₄BF₄) or fluoroboric acid (HBF₄), thus incorporating thefluoride and boron into or onto the preformed solid oxide compound inone treatment.

Another preferred method of producing the treated solid oxide compoundis to first calcine the solid oxide compound producing a calcined solidoxide compound. Then, contacting the calcined solid oxide compound withan anhydrous solution of fluoroboric acid to produced the treated solidoxide compound. Optionally, the treated solid oxide compound can befurther calcined as discussed previously in this disclosure.

The amount of fluorine present in the treated solid oxide compound isabout 1 to about 50% by weight fluorine based on the weight of thetreated solid oxide compound before calcining or the amount added to aprecalcined solid oxide compound. Preferably, it is about 3 to about 25%by weight, and most preferably, it is 4 to 25% by weight fluorine basedon the weight of the treated solid oxide compound before calcining orthe amount added to a precalcined solid oxide compound.

The compositions of this invention can be produced by contacting theorganometal compound, the treated solid oxide compound, and theorganoaluminum compound, together. This contacting can occur in avariety of ways, such as, for example, blending. Furthermore, each ofthese compounds can be fed into the reactor separately, or variouscombinations of these compounds can be contacted together before beingfurther contacted in the reactor, or all three compounds can becontacted together before being introduced into the reactor.

Currently, one method is to first contact an organometal compound and atreated solid oxide compound together, for about 1 minute to about 24hours, preferably, about 1 minute to about 1 hour, at a temperature fromabout 10° C. to about 100° C., preferably 15° C. to 50° C., to form afirst mixture, and then contact this first mixture with anorganoaluminum compound to form the catalyst composition.

Another method is to precontact the organometal compound, theorganoaluminum compound, and the treated solid oxide compound beforeinjection into a polymerization reactor for about 1 minute to about 24hours, preferably, 1 minute to 1 hour, at a temperature from about 10°C. to about 200° C., preferably 20° C. to 80° C. to produce the catalystcomposition.

A weight ratio of the organoaluminum compound to the treated solid oxidecompound in the catalyst composition ranges from about 5:1 to about1:1000, preferably, from about 3:1 to about 1:100, and most preferably,from 1:1 to 1:50.

A weight ratio of the treated solid oxide compound to the organometalcompound in the composition ranges from about 10,000:1 to about 1:1,preferably, from about 1000:1 to about 10:1, and most preferably, from250:1 to 20:1. These ratios are based on the amount of the componentscombined to give the catalyst composition.

After contacting, the catalyst composition comprises a post-contactedorganometal compound, a post-contacted organoaluminum compound, and apost-contacted treated solid oxide compound. Preferably, thepost-contacted treated solid oxide compound is the majority, by weight,of the composition. Often times, specific components of a catalyst arenot known, therefore, for this invention, the catalyst composition isdescribed as comprising post-contacted compounds.

A weight ratio of the post-contacted organoaluminum compound to thepost-contacted treated solid oxide compound in the catalyst compositionranges from about 5:1 to about 1:1000, preferably, from about 3:1 toabout 1:100, and most preferably, from 1:1 to 1:50.

A weight ratio of the post-contacted treated solid oxide compound to thepost-contacted organometal compound in the catalyst composition rangesfrom about 10,000:1 to about 1:1, preferably, from about 1000:1 to about10:1, and most preferably, from 250:1 to 20:1.

The catalyst composition of this invention has an activity greater thana catalyst composition that uses the same organometal compound, and thesame organoaluminum compound, but uses silica, fluorided silica, orsilica-boria as an activator for the organometal compound as shown incomparative examples 2-4. The activity is measured under slurrypolymerization conditions, using isobutane as the diluent, and with apolymerization temperature of about 50 to about 110° C., and an ethylenepressure of about 400 to about 800 psig. When comparing activities, thepolymerization runs should occur at the same polymerization conditions.The reactor should have substantially no indication of any wall scale,coating or other forms of fouling.

However, it is preferred if the activity is greater than about 100 gramsof polymer per gram of treated solid oxide compound per hour, morepreferably greater than about 500, and most preferably greater than1000. This activity is measured under slurry polymerization conditions,using isobutane as the diluent, and with a polymerization temperature of90° C., and an ethylene pressure of 550 psig. The reactor should havesubstantially no indication of any wall scale, coating or other forms offouling.

One of the important aspects of this invention is that no aluminoxaneneeds to be used in order to form the catalyst composition. Aluminoxaneis an expensive compound that greatly increases polymer productioncosts. This also means that no water is needed to help form suchaluminoxanes. This is beneficial because water can sometimes kill apolymerization process. Additionally, it should be noted that nofluoro-organo borate compounds need to be used in order to form thecatalyst composition. Examples of such fluoro-organo borate compoundsthat are not needed in this invention include, but are not limited to,fluorinated aryl borates, such as, N,N-dimethylaniliniumtetrakis(pentafluorophenyl)borate, triphenylcarbeniumtetrakis(pentafluorophenyl)borate, lithiumtetrakis(pentafluorophenyl)borate, tris(pentafluorophenyl)boron,N,N-dimethylanilinium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate,triphenylcarbenium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate, andmixtures thereof. The above examples and related fluoro-organo boratecompounds are thought to form “weakly-coordinating” anions when combinedwith metallocene catalysts as disclosed in U.S. Pat. No. 5,919,983. Theboron compounds of this invention are distinguished from those prior artfluoro-organo borate compounds described previously in that they areinorganic when the treated solid oxide compound is formed, eitherthrough the direct use of an inorganic borate or by calciningorganoboron compounds to boron oxides. In summary, this means that thetreated solid oxide compound, unlike the prior art fluoro-organo boratecompounds described above, is inorganic and heterogenous in diluentsduring polymerization. They can be used for polymerizing monomers andcan be easily and inexpensively produced because of the substantialabsence of any aluminoxane compounds or fluoro-organo borate compounds.Additionally, no organochromium compounds or MgCl₂ need to be added toform the invention. Although aluminoxane, fluoro-organo boratecompounds, organochromium compounds, or MgCl₂ are not needed in thepreferred embodiments to produce the catalyst composition, thesecompounds can be used in other embodiments of this invention.

In another embodiment of this invention, a process comprising contactingat least one monomer and the catalyst composition to produce at leastone polymer is provided. The term “polymer” as used in this disclosureincludes homopolymers and copolymers. The catalyst composition can beused to polymerize at least one monomer to produce a homopolymer or acopolymer. Usually, homopolymers are comprised of monomer residues,having 2 to about 20 carbon atoms per molecule, preferably 2 to about 10carbon atoms per molecule. Currently, it is preferred when at least onemonomer is selected from the group consisting of ethylene, propylene,1-butene, 3-methyl-1-butene, 1-pentene, 3-methyl-1-pentene,4-methyl-1-pentene, 1-hexene, 3-ethyl-1-hexene, 1-heptene, 1-octene,1-nonene, 1-decene, and mixtures thereof

When a homopolymer is desired, it is most preferred to polymerizeethylene or propylene. When a copolymer is desired, the copolymercomprises monomer residues and one or more comonomer residues, eachhaving from about 2 to about 20 carbon atoms per molecule. Suitablecomonomers include, but are not limited to, aliphatic 1-olefins havingfrom 3 to 20 carbon atoms per molecule, such as, for example, propylene,1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-octene, and otherolefins and conjugated or nonconjugated diolefins such as 1,3-butadiene,isoprene, piperylene, 2,3-dimethyl-1,3-butadiene, 1,4-pentadiene,1,7-hexadiene, and other such diolefins and mixtures thereof. When acopolymer is desired, it is preferred to polymerize ethylene and atleast one comonomer selected from the group consisting of 1-butene,1-pentene, 1-hexene, 1-octene, and 1-decene. The amount of comonomerintroduced into a reactor zone to produce a copolymer is generally fromabout 0.01 to about 10 weight percent comonomer based on the totalweight of the monomer and comonomer, preferably, about 0.01 to about 5,and most preferably, 0.1 to 4. Alternatively, an amount sufficient togive the above described concentrations, by weight, in the copolymerproduced can be used.

Processes that can polymerize at least one monomer to produce a polymerare known in the art, such as, for example, slurry polymerization, gasphase polymerization, and solution polymerization. It is preferred toperform a slurry polymerization in a loop reaction zone. Suitablediluents used in slurry polymerization are well known in the art andinclude hydrocarbons which are liquid under reaction conditions. Theterm “diluent” as used in this disclosure does not necessarily mean aninert material; it is possible that a diluent can contribute topolymerization. Suitable hydrocarbons include, but are not limited to,cyclohexane, isobutane, n-butane, propane, n-pentane, isopentane,neopentane, and n-hexane. Furthermore, it is most preferred to useisobutane as the diluent in a slurry polymerization. Examples of suchtechnology can be found in U.S. Pat. Nos. 4,424,341; 4,501,885;4,613,484; 4,737,280; and 5,597,892; the entire disclosures of which arehereby incorporated by reference.

The catalyst compositions used in this process produce good qualitypolymer particles without substantially fouling the reactor. When thecatalyst composition is to be used in a loop reactor zone under slurrypolymerization conditions, it is preferred when the particle size of thesolid oxide compound is in a range of about 10 to about 1000 microns,preferably about 25 to about 500 microns, and most preferably, 50 to 200microns, for best control during polymerization.

In a more specific embodiment of this invention, a process is providedto produce a catalyst composition, the process comprising (optionally,“consisting essentially of”, or “consisting of”):

-   -   (1) contacting silica with an aqueous solution containing        ammonium fluoroborate or fluoroboric acid to produce a        fluorided, boron-containing solid oxide compound having from 1        to 3 millimoles of boron per gram of fluorided, boron-containing        solid oxide compound before calcining and 4 to 25% by weight        fluorine based on the weight of the boron-containing solid oxide        compound before calcining;    -   (2) calcining the fluorided, boron-containing solid oxide        compound at a temperature within a range of 250 to 500° C. for 3        to 20 hours to produce a calcined composition;    -   (3) combining the calcined composition and        bis(n-butylcyclopentadienyl) zirconium dichloride at a        temperature within a range of 15° C. to 50° C. for 1 minute to 1        hour to produce a mixture; and    -   (4) combining the mixture and triethylaluminum to produce the        catalyst composition.

Hydrogen can be used with this invention in a polymerization process tocontrol polymer molecular weight.

After the polymers are produced, they can be formed into variousarticles, such as, for example, household containers and utensils, filmproducts, drums, fuel tanks, pipes, geomembranes, and liners. Variousprocesses can form these articles. Usually, additives and modifiers areadded to the polymer in order to provide desired effects. It is believedthat by using the invention described herein, articles can be producedat a lower cost, while maintaining most, if not all, of the uniqueproperties of polymers produced with metallocene catalysts.

EXAMPLES

Calcining

About 10 grams of an oxide compound were placed in a 1.75 inch quartztube fitted with a sintered quartz disk at the bottom. While the oxidecompound was supported on the disk, dry air was blown up through thedisk at the linear rate of about 1.6 to about 1.8 standard cubic feetper hour. An electric furnace around the quartz tube was then turned on,and the temperature was raised at the rate of about 400° C. per hour tothe indicated temperature, such as 600° C. At that temperature, theoxide compound was allowed to fluidize for three hours in the dry air.Afterward, the oxide compound was collected and stored under drynitrogen, where it was protected from the atmosphere until ready fortesting. It was never allowed to experience any exposure to theatmosphere.

Polymerization Runs

Polymerization runs were made in a 2.2 liter steel reactor equipped witha marine stirrer running at 400 revolutions per minute (rpm). Thereactor was surrounded by a steel jacket containing boiling methanolwith a connection to a steel condenser. The boiling point of themethanol was controlled by varying nitrogen pressure applied to thecondenser and jacket, which permitted precise temperature control towithin half a degree centigrade, with the help of electronic controlinstruments.

Unless otherwise stated, first, a small amount (0.01 to 0.10 gramsnormally) of an oxide compound or the inventive treated solid oxidecompound was charged under nitrogen to the dry reactor. Next, 2.0milliliters of a toluene solution containing 0.5 percent by weight ofbis(n-butylcyclopentadienyl) zirconium dichloride were added, followedby 0.6 liters of isobutane liquid. Then, 1.0 milliliter of a 1.0 molarsolution of triethylaluminum (TEA) was added, followed by another 0.6liters of isobutane liquid. The reactor was heated up to the specifiedtemperature, typically to 90° C. Finally, ethylene was added to thereactor to equal a fixed pressure of about 550 psig to produce areaction mixture. The reaction mixture was allowed to stir for usuallyabout one hour. As ethylene was consumed, more ethylene flowed in tomaintain the pressure. The activity was noted by recording the flow ofethylene into the reactor to maintain the set pressure.

After the allotted time, the ethylene flow was stopped, and the reactorslowly depressurized and opened to recover a granular polymer. In allcases, the reactor was clean with no indication of any wall scale,coating or other forms of fouling. The polymer was then removed andweighed. Activity was specified as grams of polymer produced per gram ofoxide compound or treated solid oxide compound charged per hour.

Description of Results

Control and inventive examples are described below. The results of thesepolymerization tests are listed in Tables 1 and 2.

Control Example 1 No Oxide Compound

A polymerization run was made in the absence of any oxide compound bythe procedure discussed previously. No polymer was found in the reactor,and no ethylene consumption was detected.

Control Example 2 Silica

Grade 952 silica was obtained from W.R. Grace having a pore volume ofabout 1.6 cc/g and a surface area of about 300 m²/g. A sample of thesilica was calcined at 600° C. in dry air for three hours as describedpreviously to produce a calcined silica. The calcined silica was thentested for polymerization activity with an organometal compound and TEA.The calcined silica yielded only 1 gram of polymer per gram of calcinedsilica per hour.

Control Example 3 Fluorided Silica

A 33.82 gram sample of the same grade 952 silica described in Example 2was impregnated with 70 milliliters of an aqueous solution containing3.45 grams of ammonium bifluoride to produce a fluorided silica. Then,the fluorided silica was dried under vacuum at 120° C. overnight. Asample of the fluorided silica was calcined in dry air at 450° C. forthree hours. It was then tested for polymerization activity with TEA andan organometal compound, but it yielded no polymer.

Control Example 4 Silica-Boria

A 10.3 gram sample of W.R. Grace grade 952 silica was impregnated with20 milliliters of a solution containing 0.021 moles of boric acid toproduce a silica-boria. It was then dried under vacuum at 120° C.overnight, and a sample of the silica-boria was calcined in dry air at400° C. for three hours. When tested for polymerization activity, thesilica-boria produced 12 grams of polymer per gram of silica-boria perhour.

Inventive Examples 5-7 Treated Solid Oxide Compound

A 10.3 gram sample of W.R. Grace grade 952 silica was impregnated with20 milliliters of an aqueous solution containing 0.021 moles of boricacid and 1.0 grams of ammonium bifluoride to produce a fluorided,boron-containing solid oxide compound. It was then dried under vacuum at120° C. overnight, and three different samples of the fluorided,boron-containing solid oxide compound were calcined in dry air for threehours at 300° C., 400° C., and 500° C. to produce a treated solid oxidecompound. When tested for polymerization activity, these samplesproduced 490, 305, and 161 grams of polymer per gram of treated solidoxide compound per hour respectively.

Inventive Example 8 Treated Solid Oxide Compound

A 12.5 gram sample of 12.5 grams of W.R. Grace grade 952 silica wasimpregnated with 25 milliliters of an aqueous solution containing 0.015moles of fluoroboric acid (HBF₄) to produce a fluorided,boron-containing solid oxide compound. It was then dried under vacuum at120° C. overnight, and a sample was calcined in dry air for three hoursat 250° C. to produce a treated solid oxide compound. When tested forpolymerization activity, the treated solid oxide compound produced 544grams of polymer per gram of treated solid oxide compound per hour.

Inventive Example 9 Treated Solid Oxide Compound

Four samples of grade 952 silica support were impregnated with about twotimes their weight of an aqueous solution containing varying quantitiesof ammonium fluoroborate (NH₄BF₄) to produce fluorided, boron-containingsolid oxide compounds. The exact quantities are listed in Table 2. Eachsample was then dried under vacuum at 120° C. overnight. Each of thesefluorided, boron-containing solid oxide compound samples was dividedinto smaller samples, each of which was calcined in dry air for threehours at various temperatures to produce treated solid oxide compounds.These treated solid oxide compound samples were then tested forpolymerization activity with an organometal compound and 1 millimole ofTEA. Nearly all produced polymer. Table 2 lists the various activitiesobserved.

Inventive Example 10 Treated Solid Oxide Compound

Grade 952 silica obtained from W.R. Grace was calcined in dry air at600° C. for three hours to produce a calcined silica. Then, 7.2 grams ofthe calcined silica were slurried with an ethyl ether solutioncontaining 7.2 millimoles of anhydrous fluoroboric acid (HBF4) toproduce a treated solid oxide compound. The ether was removed by blowingdry nitrogen over the slurry, and finally, the treated solid oxidecompound was warmed under flowing nitrogen to about 60° C. A 0.3283 gramsample of the treated solid oxide compound was charged to the reactorwith TEA and an organometal compound. After about 66.4 minutes, thetreated solid oxide compound produced 54 grams of polymer, giving anactivity of 150 grams of polymer per gram of treated solid oxidecompound per hour (g/g/h).

The remainder of the treated solid oxide compound was then charged tothe quartz tube for calcining and warmed under dry nitrogen to 250° C.where it was held for 3 hours. A 0.0291 gram sample was charged to thereactor with TEA and an organometal compound. After about 69.0 minutes,it produced 37 grams of polymer, giving an activity of 350 grams ofpolymer per gram of treated solid oxide compound per hour.

TABLE 1 Calcining Test Test Temp. Compound Polymer Run Time Activity*Example Compound* (° C.) (grams) (grams) (minutes) (g/g/h)  1 ControlNone 0.0000 0 61.1 0  2 Control Silica 600 0.5686 0.65 63.0 1  3 ControlFluorided Silica 450 0.4350 0 24.5 0  4 Control Silica-Boria 400 0.52364.7 45 12  5 Inventive Treated solid 300 0.0552 22 48.2 496 oxidecompound  6 Inventive Treated solid 400 0.1642 44 52.7 305 oxidecompound  7 Inventive Treated solid 500 0.1027 12 43.6 161 oxidecompound  8 Inventive Treated solid 250 0.4207 247 64.8 544 oxidecompound 10 Inventive Treated solid 600 0.3283 54 66.4 150 oxidecompound *Test Compound = oxide compound or inventive treated solidoxide compound *Activity is in units of grams of polymer per gram ofoxide compound or treated solid oxide compound per hour.

TABLE 2 (Example 9) Amount of Calcining NH₄BF₄ Temp. Silica Polymer RunTime Activity* (mmol/g*) (° C.) (grams) (grams) (minutes) (g/g/h) 0.3400 0.1088 5.2 30.0 96 0.3 550 0.1133 40.0 30.0 706 0.3 700 0.1272 1.230.0 19 0.5 200 0.0850 31.0 30.0 729 0.5 300 0.1100 37.0 30.0 673 0.5400 0.1071 50.0 30.0 934 0.5 500 0.1196 82.0 36.0 1143 0.5 600 0.103912.1 30.0 233 0.5 700 0.1220 2.3 30.0 38 1.0 550 0.1667 126.0 61.9 7331.0 450 0.0803 60.0 61.8 725 1.0 300 0.1230 39.0 18.0 1057 3.0 2800.0753 44.0 61.8 567 3.0 350 0.0523 14.0 58.5 275 3.0 450 0.0623 14.071.9 188 3.0 550 0.0542 0.0 28.0 0 *Amount of NH₄BF₄ - millimoles ofNH₄BF₄/gram of silica. *Activity - grams of polymer per gram of treatedsolid oxide compound per hour

While this invention has been described in detail for the purpose ofillustration, it is not intended to be limited thereby but is intendedto cover all changes and modifications within the spirit and scopethereof.

1. A catalyst composition comprising a contact product of an organometalcompound, an organoaluminum compound, and a treated solid oxide compoundcomprising boron, fluorine, and silica, the catalyst composition beingsubstantially free of aluminoxane compounds and compounds selected fromamong N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate,triphenylcarbenium tetrakis(pentafluorophenyl)borate, lithiumtetrakis(pentafluorophenyl)borate, tris(pentafluorophenyl)boron,N,N-dimethylanilinium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate,and triphenylcarbenium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate.2. A catalyst composition comprising: a contact product of anorganometal compound, an organoaluminum compound, and a treated solidoxide compound, the catalyst composition being substantially free ofaluminoxane compounds and compounds selected from amongN,N-dimethylanilinium tetrakis(pentafluorophenyl)borate,triphenylcarbenium tetrakis(pentafluorophenyl)borate, lithiumtetrakis(pentafluorophenyl)borate, tris(pentafluorophenyl)boron,N,N-dimethylanilinium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate,and triphenylcarbenium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate,wherein: the organometal compound has the following general formula:(X¹)(X²)(X³)(X⁴)M¹ wherein: M¹ is titanium, zirconium, or hafnium; (X¹)is a cyclopentadienyl, an indenyl, a fluorenyl, a substitutedcyclopentadienyl, a substituted indenyl, or a substituted fluorenyl; thesubstituents on the substituted cyclopentadienyl, substituted indenyl,and substituted fluorenyl of (X¹) are aliphatic groups, cyclic groups,combinations of aliphatic and cyclic groups, silyl groups, haloalkylgroups, halides, hydrogen, phosphorus groups, nitrogen groups, ororganometallic groups, wherein the organometallic groups are substitutedsilyl derivatives, substituted tin groups, substituted germanium groups,or substituted boron groups; at least one substituent on (X¹) can be abridging group which connects (X¹) and (X²); (X³) and (X⁴) areindependently halides, hydrides, aliphatic groups, substituted aliphaticgroups, cyclic groups, substituted cyclic groups, combinations ofaliphatic groups and cyclic groups, combinations of substitutedaliphatic groups and cyclic groups, combinations of aliphatic groups andsubstituted cyclic groups, combinations of substituted aliphatic groupsand substituted cyclic groups, amido groups, substituted amido groups,phosphido groups, substituted phosphido groups, alkyloxide groups,substituted alkyloxide groups, aryloxide groups, substituted aryloxidegroups, organometallic groups, or substituted organometallic groups;(X²) is a cyclopentadienyl, an indenyl, a fluorenyl, a substitutedcyclopentadienyl, a substituted indenyl, a substituted fluorenyl, ahalide, an aliphatic group, a substituted aliphatic group, a cyclicgroup, a substituted cyclic group, a combination of aliphatic groups andcyclic groups, a combination of substituted aliphatic groups and cyclicgroups, a combination of aliphatic groups and substituted cyclic groups,a combination of substituted aliphatic groups and substituted cyclicgroups, an amido group, a substituted amido group, a phosphido group, asubstituted phosphido group, an alkyloxide group, a substitutedalkyloxide group, an aryloxide group, a substituted aryloxide group, anorganometallic group, or a substituted organometallic group; thesubstituents on (X²) are aliphatic groups, cyclic groups, combinationsof aliphatic groups and cyclic groups, silyl groups, haloalkyl groups,halides, hydrogen, phosphorus groups, nitrogen groups, or organometallicgroups, wherein the organometallic groups are substituted silylderivatives, substituted tin groups, substituted germanium groups, orsubstituted boron groups; and at least one substituent on (X²) can be abridging group which connects (X¹) and (X²); the organoaluminum compoundhas the following general formula:Al(X⁵)_(n)(X⁶)_(3−n) wherein: (X⁵) is a hydrocarbyl having from 1 toabout 20 carbon atoms; (X⁶) is a halide, hydride, or alkoxide; and “n”is a number from 1 to 3 inclusive; and the treated solid oxide compoundcomprises fluorine, boron, and silica.
 3. The catalyst composition asclaimed in claim 2, wherein the catalyst composition has an activitygreater than 500 grams of polymer per gram of treated solid oxidecompound per hour under slurry polymerization conditions, usingisobutane as a diluent, with a polymerization temperature of 90° C., andan ethylene pressure of 550 psig.
 4. The catalyst composition as claimedin claim 2, wherein the catalyst composition has an activity greaterthan 1000 grams of polymer per gram of treated solid oxide compound perhour under slurry polymerization conditions, using isobutane as adiluent, with a polymerization temperature of 90° C., and an ethylenepressure of 550 psig.
 5. The catalyst composition as claimed in claim 2,wherein the weight ratio of the organoaluminum compound to the treatedsolid oxide compound in the catalyst composition ranges from about 3:1to about 1:100.
 6. The catalyst composition as claimed in claim 2,wherein the weight ratio of the organoaluminum compound to the treatedsolid oxide compound in the catalyst composition ranges from 1:1 to1:50.
 7. The catalyst composition as claimed in claim 2, wherein theweight ratio of the treated solid oxide compound to the organometalcompound in the catalyst composition ranges from about 1000:1 to about10:1.
 8. The catalyst composition as claimed in claim 2, wherein theweight ratio of the treated solid oxide compound to the organometalcompound in the catalyst composition ranges from 250:1 to 20:1.
 9. Thecatalyst composition as claimed in claim 2, wherein the organometalcompound is bis(cyclopentadienyl)hafnium dichloride,bis(cyclopentadienyl)zirconium dichloride,1,2-ethanediylbis(η⁵-1-indenyl)di-n-butoxyhafnium,1,2-ethanediylbis(η⁵-1-indenyl)dimethylzirconium,3,3-pentanediylbis(η⁵-4,5,6,7-tetrahydro-1-indenytl)hafnium dichloride,methylphenylsilylbis(η⁵-4,5,6,7-tetrahydro-1-indenyl)zirconiumdichloride, bis(n-butylcyclopentadienyl)bis(di-t-butylamido)hafnium,bis(n-butylcyclopentadienyl)zirconium dichloride,dimethylsilylbis(1-indenyl)zirconium dichloride,octylphenylsilylbis(1-indenyl)hafnium dichloride,dimethylsilylbis(η⁵-4,5,6,7-tetrahydro-1-indenyl)zirconium dichloride,dimethylsilylbis(2-methyl-1-indenyl)zirconium dichloride,1,2-ethanediylbis(9-fluorenyl)zirconium dichloride, indenyl diethoxytitanium(IV) chloride,(isopropylamidodimethylsilyl)cyclopentadienyltitanium dichloride,bis(pentamethylcyclopentadienyl)zirconium dichloride,bis(indenyl)zirconium dichloride, or methyloctylsilylbis(9-fluorenyl)zirconium dichloride.
 10. The catalyst composition asclaimed in claim 2, wherein the organometal compound isbis(n-butylcyclopentadienyl)zirconium dichloride, bis(indenyl) zirconiumdichloride, dimethylsilylbis(1-indenyl)zirconium dichloride, ormethyloctylsilyl bis(9-fluorenyl)zirconium dichloride.
 11. The catalystcomposition as claimed in claim 2, wherein the organoaluminum compoundis trimethylaluminum, triethylaluminum, tripropylaluminum,diethylaluminum ethoxide, tributylaluminum, diisobutylaluminum hydride,triisobutylaluminum, or diethylaluminum chloride.
 12. The catalystcomposition as claimed in claim 2, wherein the organoaluminum compoundis triethylaluminum.
 13. The catalyst composition as claimed in claim 1,wherein the organometal compound has the following general formula:(X¹)(X²)(X³)(X⁴)M¹ wherein: M¹ is titanium, zirconium, or hafnium; (X¹)is a cyclopentadienyl, an indenyl, a fluorenyl, a substitutedcyclopentadienyl, a substituted indenyl, or a substituted fluorenyl; thesubstituents on the substituted cyclopentadienyl, substituted indenyl,and substituted fluorenyl of (X¹) are aliphatic groups, cyclic groups,combinations of aliphatic and cyclic groups, silyl groups, haloalkylgroups, halides, hydrogen, phosphorus groups, nitrogen groups, ororganometallic groups, wherein the organometallic groups are substitutedsilyl derivatives, substituted tin groups, substituted germanium groups,or substituted boron groups; at least one substituent on (X¹) can be abridging group which connects (X¹) and (X²); (X³) and (X⁴) areindependently halides, hydrides, aliphatic groups, substituted aliphaticgroups, cyclic groups, substituted cyclic groups, combinations ofaliphatic groups and cyclic groups, combinations of substitutedaliphatic groups and cyclic groups, combinations of aliphatic groups andsubstituted cyclic groups, combinations of substituted aliphatic groupsand substituted cyclic groups, amido groups, substituted amido groups,phosphido groups, substituted phosphido groups, alkyloxide groups,substituted alkyloxide groups, aryloxide groups, substituted aryloxidegroups, organometallic groups, or substituted organometallic groups;(X²) is a cyclopentadienyl, an indenyl, a fluorenyl, a substitutedcyclopentadienyl, a substituted indenyl, a substituted fluorenyl, ahalide, an aliphatic group, a substituted aliphatic group, a cyclicgroup, a substituted cyclic group, a combination of aliphatic groups andcyclic groups, a combination of substituted aliphatic groups and cyclicgroups, a combination of aliphatic groups and substituted cyclic groups,a combination of substituted aliphatic groups and substituted cyclicgroups, an amido group, a substituted amido group, a phosphido group, asubstituted phosphido group, an alkyloxide group, a substitutedalkyloxide group, an aryloxide group, a substituted aryloxide group, anorganometallic group, or a substituted organometallic group; thesubstituents on (X²) are aliphatic groups, cyclic groups, combinationsof aliphatic groups and cyclic groups, silyl groups, haloalkyl groups,halides, hydrogen, phosphorus groups, nitrogen groups, or organometallicgroups, wherein the organometallic groups are substituted silylderivatives, substituted tin groups, substituted germanium groups, orsubstituted boron groups; and at least one substituent on (X²) can be abridging group which connects (X¹) and (X²).
 14. The catalystcomposition as claimed in claim 1, wherein the organoaluminum compoundhas the following general formula:Al(X⁵)_(n)(X⁶)_(3−n) wherein: (X⁵) is a hydrocarbyl having from 1 toabout 20 carbon atoms; (X⁶) is a halide, hydride, or alkoxide; and “n”is a number from 1 to 3 inclusive.
 15. A catalyst compositioncomprising: a contact product of an organometal compound, anorganoaluminum compound, and a treated solid oxide compound, wherein:the organometal compound has the following general formula:(X¹)(X²)(X³)(X⁴)M¹ wherein: M¹ is titanium, zirconium, or hafnium; (X¹)is a cyclopentadienyl, an indenyl, a fluorenyl, a substitutedcyclopentadienyl, a substituted indenyl, or a substituted fluorenyl; thesubstituents on the substituted cyclopentadienyl, substituted indenyl,and substituted fluorenyl of (X¹) are aliphatic groups, cyclic groups,combinations of aliphatic and cyclic groups, silyl groups, haloalkylgroups, halides, hydrogen, phosphorus groups, nitrogen groups, ororganometallic groups, wherein the organometallic groups are substitutedsilyl derivatives, substituted tin groups, substituted germanium groups,or substituted boron groups; at least one substituent on (X¹) can be abridging group which connects (X¹) and (X²); (X³) and (X⁴) areindependently halides, hydrides, aliphatic groups, substituted aliphaticgroups, cyclic groups, substituted cyclic groups, combinations ofaliphatic groups and cyclic groups, combinations of substitutedaliphatic groups and cyclic groups, combinations of aliphatic groups andsubstituted cyclic groups, combinations of substituted aliphatic groupsand substituted cyclic groups, amido groups, substituted amido groups,phosphido groups, substituted phosphido groups, alkyloxide groups,substituted alkyloxide groups, aryloxide groups, substituted aryloxidegroups, organometallic groups, or substituted organometallic groups;(X²) is a cyclopentadienyl, an indenyl, a fluorenyl, a substitutedcyclopentadienyl, a substituted indenyl, a substituted fluorenyl, ahalide, an aliphatic group, a substituted aliphatic group, a cyclicgroup, a substituted cyclic group, a combination of aliphatic groups andcyclic groups, a combination of substituted aliphatic groups and cyclicgroups, a combination of aliphatic groups and substituted cyclic groups,a combination of substituted aliphatic groups and substituted cyclicgroups, an amido group, a substituted amido group, a phosphido group, asubstituted phosphido group, an alkyloxide group, a substitutedalkyloxide group, an aryloxide group, a substituted aryloxide group, anorganometallic group, or a substituted organometallic group; thesubstituents on (X²) are aliphatic groups, cyclic groups, combinationsof aliphatic groups and cyclic groups, silyl groups, haloalkyl groups,halides, hydrogen, phosphorus groups, nitrogen groups, or organometallicgroups, wherein the organometallic groups are substituted silylderivatives, substituted tin groups, substituted germanium groups, orsubstituted boron groups; and at least one substituent on (X²) can be abridging group which connects (X¹) and (X²); the organoaluminum compoundhas the following general formula:Al(X⁵)_(n)(X⁶)_(3−n) wherein: (X⁵) is a hydrocarbyl having from 1 toabout 20 carbon atoms; (X⁶) is a halide, hydride, or alkoxide; and “n”is a number from 1 to 3 inclusive; the treated solid oxide compoundcomprises fluorine, boron, and silica; and the catalyst composition hasa polymerization activity greater than 100 grams of polymer per gram oftreated solid oxide compound per hour under slurry polymerizationconditions, using isobutane as a diluent, with a polymerizationtemperature of 90° C., and an ethylene pressure of 550 psig, thecatalyst composition being substantially free of aluminoxane compoundsand compounds selected from among N,N-dimethylaniliniumtetrakis(pentafluorophenyl)borate, triphenylcarbeniumtetrakis(pentafluorophenyl)borate, lithiumtetrakis(pentafluorophenyl)borate, tris(pentafluorophenyl)boron,N,N-dimethylanilinium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate,and triphenylcarbenium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate.16. A catalyst composition comprising a contact product of anorganometal compound, an organoaluminum compound, and a treated solidoxide compound comprising boron, fluorine, and a solid oxide compound,wherein the catalyst composition is substantially free of aluminoxanecompounds and compounds selected from among N,N-dimethylaniliniumtetrakis(pentafluorophenyl)borate, triphenylcarbeniumtetrakis(pentafluorophenyl)borate, lithiumtetrakis(pentafluorophenyl)borate, tris(pentafluorophenyl)boron,N,N-dimethylanilinium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate,and triphenylcarbenium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate;and wherein the amount of boron in the treated solid oxide compound,prior to contacting, is in the range of about 0.1 to about 10 millimolesof boron per gram of treated solid oxide.
 17. A catalyst compositioncomprising: a contact product of an organometal compound, anorganoaluminum compound, and a calcined treated solid oxide compound,the catalyst composition being substantially free of aluminoxanecompounds and compounds selected from among N,N-dimethylaniliniumtetrakis(pentafluorophenyl)borate, triphenylcarbeniumtetrakis(pentafluorophenyl)borate, lithiumtetrakis(pentafluorophenyl)borate, tris(pentafluorophenyl)boron,N,N-dimethylanilinium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate,and triphenylcarbenium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate,wherein: the organometal compound has the following general formula:(X¹)(X²)(X³)(X⁴)M¹ wherein: M¹ is titanium, zirconium, or hafnium; (X¹)is a cyclopentadienyl, an indenyl, a fluorenyl, a substitutedcyclopentadienyl, a substituted indenyl, or a substituted fluorenyl; thesubstituents on the substituted cyclopentadienyl, substituted indenyl,and substituted fluorenyl of (X¹) are aliphatic groups, cyclic groups,combinations of aliphatic and cyclic groups, silyl groups, haloalkylgroups, halides, hydrogen, phosphorus groups, nitrogen groups, ororganometallic groups, wherein the organometallic groups are substitutedsilyl derivatives, substituted tin groups, substituted germanium groups,or substituted boron groups; at least one substituent on (X¹) can be abridging group which connects (X¹) and (X²); (X³) and (X⁴) areindependently halides, hydrides, aliphatic groups, substituted aliphaticgroups, cyclic groups, substituted cyclic groups, combinations ofaliphatic groups and cyclic groups, combinations of substitutedaliphatic groups and cyclic groups, combinations of aliphatic groups andsubstituted cyclic groups, combinations of substituted aliphatic groupsand substituted cyclic groups, amido groups, substituted amido groups,phosphido groups, substituted phosphido groups, alkyloxide groups,substituted alkyloxide groups, aryloxide groups, substituted aryloxidegroups, organometallic groups, or substituted organometallic groups;(X²) is a cyclopentadienyl, an indenyl, a fluorenyl, a substitutedcyclopentadienyl, a substituted indenyl, a substituted fluorenyl, ahalide, an aliphatic group, a substituted aliphatic group, a cyclicgroup, a substituted cyclic group, a combination of aliphatic groups andcyclic groups, a combination of substituted aliphatic groups and cyclicgroups, a combination of aliphatic groups and substituted cyclic groups,a combination of substituted aliphatic groups and substituted cyclicgroups, an amido group, a substituted amido group, a phosphido group, asubstituted phosphido group, an alkyloxide group, a substitutedalkyloxide group, an aryloxide group, a substituted aryloxide group, anorganometallic group, or a substituted organometallic group; thesubstituents on (X²) are aliphatic groups, cyclic groups, combinationsof aliphatic groups and cyclic groups, silyl groups, haloalkyl groups,halides, hydrogen, phosphorus groups, nitrogen groups, or organometallicgroups, wherein the organometallic groups are substituted silylderivatives, substituted tin groups, substituted germanium groups, orsubstituted boron groups; and at least one substituent on (X²) can be abridging group which connects (X¹) and (X²); the organoaluminum compoundhas the following general formula:Al(X⁵)_(n)(X⁶)_(3−n) wherein: (X⁵) is a hydrocarbyl having from 1 toabout 20 carbon atoms; (X⁶) is a halide, hydride, or alkoxide; and “n”is a number from 1 to 3 inclusive; the treated solid oxide compoundcomprises fluorine, boron, and a solid oxide compound; and the amount ofboron in the treated solid oxide compound, prior to calcining, is in therange of about 0.1 to about 10 millimoles of boron per gram of treatedsolid oxide.
 18. A catalyst composition comprising: a contact product ofan organometal compound, an organoaluminum compound, and a calcinedtreated solid oxide compound, wherein: the organometal compound has thefollowing general formula:(X¹)(X²)(X³)(X⁴)M¹ wherein: M¹ is titanium, zirconium, or hafnium; (X¹)is a cyclopentadienyl, an indenyl, a fluorenyl, a substitutedcyclopentadienyl, a substituted indenyl, or a substituted fluorenyl; thesubstituents on the substituted cyclopentadienyl, substituted indenyl,and substituted fluorenyl of (X¹) are aliphatic groups, cyclic groups,combinations of aliphatic and cyclic groups, silyl groups, haloalkylgroups, halides, hydrogen, phosphorus groups, nitrogen groups, ororganometallic groups, wherein the organometallic groups are substitutedsilyl derivatives, substituted tin groups, substituted germanium groups,or substituted boron groups; at least one substituent on (X¹) can be abridging group which connects (X¹) and (X²); (X³) and (X⁴) areindependently halides, hydrides, aliphatic groups, substituted aliphaticgroups, cyclic groups, substituted cyclic groups, combinations ofaliphatic groups and cyclic groups, combinations of substitutedaliphatic groups and cyclic groups, combinations of aliphatic groups andsubstituted cyclic groups, combinations of substituted aliphatic groupsand substituted cyclic groups, amido groups, substituted amido groups,phosphido groups, substituted phosphido groups, alkyloxide groups,substituted alkyloxide groups, aryloxide groups, substituted aryloxidegroups, organometallic groups, or substituted organometallic groups;(X²) is a cyclopentadienyl, an indenyl, a fluorenyl, a substitutedcyclopentadienyl, a substituted indenyl, a substituted fluorenyl, ahalide, an aliphatic group, a substituted aliphatic group, a cyclicgroup, a substituted cyclic group, a combination of aliphatic groups andcyclic groups, a combination of substituted aliphatic groups and cyclicgroups, a combination of aliphatic groups and substituted cyclic groups,a combination of substituted aliphatic groups and substituted cyclicgroups, an amido group, a substituted amido group, a phosphido group, asubstituted phosphido group, an alkyloxide group, a substitutedalkyloxide group, an aryloxide group, a substituted aryloxide group, anorganometallic group, or a substituted organometallic group; thesubstituents on (X²) are aliphatic groups, cyclic groups, combinationsof aliphatic groups and cyclic groups, silyl groups, haloalkyl groups,halides, hydrogen, phosphorus groups, nitrogen groups, or organometallicgroups, wherein the organometallic groups are substituted silylderivatives, substituted tin groups, substituted germanium groups, orsubstituted boron groups; and at least one substituent on (X²) can be abridging group which connects (X¹) and (X²); the organoaluminum compoundhas the following general formula:Al(X⁵)_(n)(X⁶)_(3−n) wherein: (X⁵) is a hydrocarbyl having from 1 toabout 20 carbon atoms; (X⁶) is a halide, hydride, or alkoxide; and “n”is a number from 1 to 3 inclusive; the treated solid oxide compoundcomprises fluorine, boron, and a solid oxide compound; the amount ofboron in the treated solid oxide compound, prior to calcining, is in therange of about 0.1 to about 10 millimoles of boron per gram of treatedsolid oxide; and the catalyst composition has a polymerization activitygreater than 100 grams of polymer per gram of treated solid oxidecompound per hour under slurry polymerization conditions, usingisobutane as a diluent, with a polymerization temperature of 90° C., andan ethylene pressure of 550 psig, the catalyst composition beingsubstantially free of aluminoxane compounds and compounds selected fromamong N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate,triphenylcarbenium tetrakis(pentafluorophenyl)borate, lithiumtetrakis(pentafluorophenyl)borate, tris(pentafluorophenyl)boron,N,N-dimethylanilinium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate,and triphenylcarbenium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate.19. The catalyst composition as claimed in claim 18, wherein thecatalyst composition has an activity greater than 500 grams of polymerper gram of treated solid oxide compound per hour under slurrypolymerization conditions, using isobutane as a diluent, with apolymerization temperature of 90° C., and an ethylene pressure of 550psig.
 20. The catalyst composition as claimed in claim 18, wherein thecatalyst composition has an activity greater than 1000 grams of polymerper gram of treated solid oxide compound per hour under slurrypolymerization conditions, using isobutane as a diluent, with apolymerization temperature of 90° C., and an ethylene pressure of 550psig.
 21. A catalyst composition comprising a contact product of anorganometal compound, an organoaluminum compound, and a treated solidoxide compound comprising boron, fluorine, and silica, wherein thecatalyst composition is substantially free of aluminoxane compounds andcompounds selected from among N,N-dimethylaniliniumtetrakis(pentafluorophenyl)borate, triphenylcarbeniumtetrakis(pentafluorophenyl)borate, lithiumtetrakis(pentafluorophenyl)borate, tris(pentafluorophenyl)boron,N,N-dimethylanilinium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate,and triphenylcarbenium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate;and wherein the catalyst composition has an activity greater than 100grams of polymer per gram of treated solid oxide compound per hour underslurry polymerization conditions, using isobutane as a diluent, with apolymerization temperature of 90° C., and an ethylene pressure of 550psig.
 22. The catalyst composition of claim 21, consisting essentiallyof the contact product of the organometal compound, the organoaluminumcompound, and the treated solid oxide compound comprising boron,fluorine, and silica.